Accelerated Development Program (Start ASAP)

Cagayan State University; Philippines; Hybrid; PHP 300,000 - 420,000; Full time

Job summary

Cognizant is hiring a Pharmacovigilance Associate in a hybrid, rotational shift role to monitor drug safety data and support pharma R&D.

You will monitor safety data, collaborate with cross-functional teams, and analyze adverse events to inform risk management. The position emphasizes PV process improvements and regulatory compliance, with ongoing training to stay current in the field.

Qualifications

• Excellent communication skills to collaborate with diverse teams.
• Attention to detail in documenting safety-related activities.
• Adaptability to rotational shifts and hybrid work model.

Responsibilities

• Monitor and assess drug safety data to ensure regulatory compliance.
• Collaborate with cross-functional teams to enhance pharmacovigilance processes.
• Analyze adverse event reports and provide insights for risk management strategies.
• Support the development of safety protocols and guidelines for pharmaceutical products.
• Conduct literature research to identify potential safety concerns and propose solutions.
• Assist in preparation of safety reports for regulatory submissions.
• Participate in training sessions to stay updated on PV trends.
• Contribute to continuous improvement of PV systems and methodologies.

Skills

Attention to detail

Communication skills

Adaptability

Job description

Join Cognizant as a Pharmacovigilance Associate to monitor drug safety data and support pharma R&D in a hybrid, rotational shift role.

Your Role

Key responsibilities include:

• Monitor and assess drug safety data to ensure compliance with regulatory standards
• Collaborate with cross-functional teams to enhance pharmacovigilance processes
• Analyze adverse event reports and provide insights for risk management strategies
• Support the development of safety protocols and guidelines for pharmaceutical products
• Conduct thorough research to identify potential safety concerns and recommend solutions
• Assist in the preparation of safety reports for submission to regulatory authorities
• Utilize Pharma Research & Development skills to improve case processing efficiency
• Participate in training sessions to stay updated on industry best practices
• Contribute to the continuous improvement of pharmacovigilance systems and methodologies
• Ensure accurate documentation of all safety-related activities and findings
• Facilitate communication between stakeholders to address safety issues promptly
• Implement strategies to enhance the quality and reliability of safety data
• Provide technical support in the analysis and interpretation of complex safety data

About You

The company is looking for:

• 0 - 1 years of experience in Pharma Research & Development
• Proficiency in Pharma Research & Development with a focus on safety data analysis
• Knowledge of PV Case Processing and its impact on drug safety
• Familiarity with regulatory requirements related to pharmacovigilance
• Excellent communication skills to collaborate with diverse teams
• Attention to detail in documenting safety-related activities
• Adaptability to rotational shifts and hybrid work model
• Eagerness to learn and stay updated on pharmacovigilance trends